CNR Institutional Research Information System

D'ESPOSITO, MAURIZIO
 Distribuzione geografica
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Continente #
AS - Asia 2.582
NA - Nord America 1.826
EU - Europa 695
SA - Sud America 505
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 18
Totale 5.688
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Nazione #
US - Stati Uniti d'America 1.725
SG - Singapore 1.083
CN - Cina 516
BR - Brasile 387
HK - Hong Kong 308
IT - Italia 249
VN - Vietnam 244
FR - Francia 151
BD - Bangladesh 112
KR - Corea 106
DE - Germania 71
NL - Olanda 67
IN - India 43
GB - Regno Unito 42
CA - Canada 41
JP - Giappone 34
AR - Argentina 28
CO - Colombia 24
MX - Messico 23
EC - Ecuador 20
FI - Finlandia 20
ZA - Sudafrica 20
ID - Indonesia 17
IQ - Iraq 15
TR - Turchia 15
CL - Cile 13
PL - Polonia 12
SA - Arabia Saudita 12
ES - Italia 11
VE - Venezuela 11
MA - Marocco 10
MY - Malesia 10
PY - Paraguay 10
IL - Israele 9
RU - Federazione Russa 9
UZ - Uzbekistan 9
TH - Thailandia 8
AT - Austria 7
CR - Costa Rica 7
EG - Egitto 7
JM - Giamaica 7
UA - Ucraina 7
CZ - Repubblica Ceca 6
HN - Honduras 6
PK - Pakistan 6
AE - Emirati Arabi Uniti 5
GR - Grecia 5
JO - Giordania 5
KE - Kenya 5
LT - Lituania 5
SE - Svezia 5
AL - Albania 4
AZ - Azerbaigian 4
BO - Bolivia 4
DZ - Algeria 4
GT - Guatemala 4
IE - Irlanda 4
KZ - Kazakistan 3
PE - Perù 3
PR - Porto Rico 3
RO - Romania 3
TN - Tunisia 3
UY - Uruguay 3
BG - Bulgaria 2
BW - Botswana 2
CH - Svizzera 2
ET - Etiopia 2
GY - Guiana 2
HR - Croazia 2
HU - Ungheria 2
KG - Kirghizistan 2
KW - Kuwait 2
LB - Libano 2
NP - Nepal 2
PH - Filippine 2
RS - Serbia 2
ZM - Zambia 2
AM - Armenia 1
AO - Angola 1
AW - Aruba 1
BB - Barbados 1
BE - Belgio 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CG - Congo 1
CI - Costa d'Avorio 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GD - Grenada 1
GE - Georgia 1
GP - Guadalupe 1
KH - Cambogia 1
LV - Lettonia 1
MD - Moldavia 1
ML - Mali 1
MM - Myanmar 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
Totale 5.661
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Città #
Singapore 650
Santa Clara 384
Hong Kong 304
San Jose 225
Hefei 211
Ashburn 164
Lauterbourg 115
Ho Chi Minh City 104
Seoul 103
Los Angeles 96
Beijing 87
Hanoi 58
Frankfurt am Main 44
Naples 43
Dallas 35
São Paulo 33
Buffalo 32
New York 32
Rome 24
Milan 22
Tokyo 20
Brooklyn 19
Rio de Janeiro 15
Atlanta 13
Avellino 13
Curitiba 13
Orem 12
Chicago 11
Turners Falls 11
Aversa 10
Helsinki 10
Minamishinagawa 10
Da Nang 9
Denver 9
Dhaka 9
Haiphong 9
Manchester 9
Montreal 9
Phoenix 9
Tashkent 9
Baghdad 8
Bogotá 8
Brasília 8
Chennai 8
Cleveland 8
Guangzhou 8
Jacksonville 8
Johannesburg 8
Toronto 8
Bologna 7
Campinas 7
Fortaleza 7
London 7
Newark 7
San Francisco 7
Warsaw 7
Amsterdam 6
Belo Horizonte 6
Guayaquil 6
Houston 6
Jeddah 6
Munich 6
Turin 6
Turku 6
Athens 5
Bari 5
Boston 5
Cairo 5
Charlotte 5
Council Bluffs 5
Figino 5
Istanbul 5
Kingston 5
Malang 5
Medellín 5
Memphis 5
Nairobi 5
Palermo 5
Porto Alegre 5
Redondo Beach 5
San José 5
Amman 4
Asunción 4
Baku 4
Bengaluru 4
Birmingham 4
Cape Town 4
Cincinnati 4
Dublin 4
Düsseldorf 4
Elk Grove Village 4
Florence 4
Franca 4
Goiânia 4
Karachi 4
Kuala Lumpur 4
Lafayette 4
Lappeenranta 4
Mauá 4
Mexico City 4
Totale 3.325
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Nome #
Epigenetic control of hypoxia inducible factor-1?-dependent expression of placental growth factor in hypoxic conditions 104
X inactivation and reactivation in X-linked diseases 103
Deep Insights Into Mecp2-Driven Transcriptional (De)Regulation At Embryonic Developmental Stage Through RNA-Seq Data Analysis 100
The evolutionary history of the second pseudoautosomal region revised 99
F(2)-dihomo-isoprostanes as potential early biomarkers of lipid oxidative damage in Rett syndrome 89
MULTI-OMICS ANALYSIS SHEDS LIGHT ON HOW SHELF-LIFE OF TOMATO FRUIT IS PROLONGED 85
Multi-omics data integration provides insights into the post-harvest biology of a long shelf-life tomato landrace 80
Glycosphingolipid metabolic reprogramming drives neural differentiation 79
F(4)-neuroprostanes mediate neurological severity in Rett syndrome. 79
ZFP57/KAP1 Genomic Association and Targeted Epigenetic Regulation at Imprinted and Not Imprinted Loci 70
Genomic and epigenomic analysis of tomato fruit senescence 70
GENOME-WIDE ANALYSIS OF HISTONE MODIFICATIONS AND ASSOCIATION WITH RIPENING-RELATED GENES DURING POST-HARVEST IN TOMATO FRUIT 68
Alternative splicing of the human gene SYBL1 modulates protein domain architecture of longin VAMP7/TI-VAMP, showing both non-SNARE and synaptobrevin-like isoforms. 66
A dual mechanism controlling the localization and function of exocytic v-SNAREs 65
Vamp7 63
Retention of Mitochondria in Mature Human Red Blood Cells as the Result of Autophagy Impairment in Rett Syndrome 63
A Multi-Omics approach to get insights into fruit senescence regulatory networks in a tomato landrace with long shelf-life. 63
Agonist stimulated 5-HT7R recovers gene expression profile in cortical neurons of a Rett syndrome mouse model 63
Select item 10671Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online. 62
MECP2, a multi-talented modulator of chromatin architecture 61
Transcriptomic and epigenomic landscape in rett syndrome 61
INSIGHTS INTO FRUIT SENESCENCE REGULATORY NETWORKS IN A TOMATO LANDRACE WITH LONG SHELF-LIFE 61
Genetic variability at the second pseudoautosomal region in ancient and modern humans 60
Global transcriptome profiles of italian mediterranean buffalo embryos with normal and retarded growth. 59
Minimally Invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 58
O6-methylguanine-DNA methyltransferase in equine sarcoids: molecular and epigenetic analysis. 58
CODING AND NON-CODING RNAS IN A LONG SHELF-LIFE TOMATO VARIETY 58
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing. 58
Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling 57
Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E 54
DNA methylation in X inactivation, imprinting and associated diseases 54
In vivo analysis of DNA methylation patterns recognized by specific proteins: coupling chromatin immunoprecipitation and bisulfite genomic sequencing 53
Genomic characterization and chromosomal mapping of 5 river buffalo skeletal muscle differentiation master genes 53
The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients 53
Early oxidative damage in Rett mouse brain 51
Differential DNA Methylation as a Tool for Non-Invasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies 51
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome 51
Multi-Omics analysis of tomato fruit senescence 51
An autoregulatory loop mediated by miR-21 and PDCD4 controls the AP-1 activity in RAS transformation 49
Human synaptobrevin like 1 gene basal transcription is regulated through the interaction of Staf-ZNF143 factors with evolutionary conserved Cis-elements 49
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome 48
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region 48
Expressed STSs and transcription of human Xq28. 47
Physical mappaing of a retinal-specific trascription factor and the epigenetic mark H3K9me3 correlated to rhodopsin and genome wide retinal loci. 47
DDX11L: a novel transcript family emerging from human subtelomeric regions 47
Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes. 47
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications 46
Folate treatment and unbalanced methylation and changes of allelic expression induced by hyperhomocysteinaemia in patients with uraemia. 46
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 46
Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region 46
Abnormal N-glycosylation pattern for brain nucleotide pyrophosphatase-5 (NPP-5) in Mecp2-mutant murine models of Rett syndrome. 45
Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome 45
Molecular dissection of two human chromatin diseases, Rett syndrome and ICF syndrome 45
Partial rescue of Rett syndrome by omega-3 polyunsaturated fatty acids (PUFAs) oil 44
Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease. 44
Reduced brain UCP2 expression mediated by microRNA-503 contributes to increased stroke susceptibility in the high-salt fed stroke-prone spontaneously hypertensive rat 44
Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21 -> q22 43
Longins and their longins domains:regulated SNAREs and multifunctional SNARE regulators 43
MECP2 Duplication Syndrome: Evidence of Enhanced Oxidative Stress. A Comparison with Rett Syndrome 42
Non-coding RNAs in chromatin disease involving neurological defects 42
Epigenetic regulation of hypoxia-induced PlGF expression 41
VAMP subfamilies identified by specific R-SNARE motifs 41
From sequence analysis to diseases identification in the distal human xq28 41
Molecular and epigenetic analysis of the fragile histidine triad tumour suppressor gene in equine sarcoids 41
Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease 40
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome 40
Anti-Mullerian hormone (AMH) concentration in follicular fluid and mRNA expression of AMH receptor type II and LH receptor in granulosa cells as predictive markers of good buffalo (Bubalus bubalis) donors 39
Complex Events In The Evolution Of The Human Pseudoautosomal Region 2 (PAR2) 39
Role of Mecp2 in the High-Order Chromatin Structure During Neural Differentiation 37
Gene Expression Profile in Liver Transplantation and the Influence of Gene Dysregulation Occurring in Deceased Donor Grafts 37
Expression of HOX homeogenes in human neuroblastoma cell culture lines. 36
Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples 36
Chromosome territory re-organisation in a human disease with altered DNA methylation 36
4. Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene 36
Molecular analysis of the heterogeneity region of the human ribosomal spacer. 36
Epigenetic control of hypoxia-induced Placental Growth Factor expression 36
Multiple binding of methyl-CpG and polycomb proteins in long-term gene silencing events 36
Chapter 18. Non-invasive Prenatal Diagnosis: An epigenetic approach to the detection of common fetal chromosome disorders by analysis of maternal blood samples. 35
Expression of HOX homeogenes in human neuroblastoma cell culture lines 35
Relationships between MeCP2 and pericentric heterochromatin factors during neural differentiation 35
The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. 35
Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications 34
MeCP2 as a genome-wide modulator: the renewal of an old story. 34
DNA methylation 40 years later: its role in human health and disease 33
MeCP2 transcription analysis and X-inactivation pattern in a Rett girl brain tissue. 32
Variegated silencing through epigenetic modifications of a large Xq region in a case of balanced X;2 translocation with Incontinentia Pigmenti-like phenotype. 32
ATRX contributes to MECP2-mediated pericentric heterochromatin organization during neural differentiation 32
A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line 32
Molecular dissection of two human chromatin disease, Rett syndrome and ICF syndrome 32
Two human homeobox genes. c1 and c8: structure analysis and expression in embryonic development. 31
Partial rescue of Rett syndrome by omega-3 polyunsaturated fatty acids (PUFAs) oil 31
Involvement of PGC-1, NRF-1, and NRF-2 in metabolic response by rat liver to hormonal and environmental signals 31
Epigenomic and transcriptional effects of Dnmt3b mutations in human ICF syndrome-derived B cell lines. 30
High resolution methylation analysis of HMLH1 promoter in sporadic endometrial and colorectal carcinomas. 30
MeCP2 is required for major satellite forward transcript recruitment at pericentric heterochromatin during neural differentiation 30
Second Human Peudoautosomal Region: Biology, Genes and Implication for the Pathogenesis of Rett Syndrome 30
EPITOM: an integrated study of epigenomics in tomato fruit during post-harvest 30
Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome. 30
DNA METHYLATION IN TRANSCRIPTIONAL REPRESSION OF TWO DIFFERENTIALLY EXPRESSED X-LINKED GENES, GPC3 AND SYBL1 30
Scavenger Receptor B1 oxidative post-translational modifications are responsible for its loss in Rett syndrome 29
Totale 4.917
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Categoria #
all - tutte 19.608
article - articoli 13.842
book - libri 91
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 525
Totale 34.066
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202431 0 0 0 0 0 0 0 0 2 0 28 1
2024/20251.810 32 9 150 75 347 51 8 88 51 80 494 425
2025/20263.108 157 256 278 474 525 167 472 150 147 176 151 155
2026/2027739 211 157 371 0 0 0 0 0 0 0 0 0
Totale 5.688